Clinical Nurse_Care Coordinator

Why Planned Parenthood?

Working at Planned Parenthood Great Northwest, Hawai'i, Alaska, Indiana, Kentucky is more than a job. It provides the opportunity to contribute to our powerful mission and perform meaningful work.

In healthcare services, this means a commitment to providing the absolute best in patient care and education. Our exceptional health center staff drives our mission forward by upholding our acclaimed customer service & confidentiality standards, and working to create a safe, judgement-free space for anyone seeking Planned Parenthood services.

About our Clinical Nurse Care Coordinator position

Serves as the primary study coordinator for specific studies and assists with the implementation of other studies as needed. Recruits, screens, schedules, and enrolls research subjects and ensures accurate data collection and entry. Provides support on research related projects. Participate in study startup, monitoring activities, and closeout. Responsible for maintaining study regulatory documents and binders. Performs patient care responsibilities within job scope and as required for study tasks. What will you be doing! Coordinates and provides support to research-related projects in conjunction with the Clinical Research Manager, Director of Research/PI. Contributes to research study planning and implementation for specific studies according to required protocols. Acts as Research Coordinator on a variety of studies at multiple locations as needed. Activities include recruitment, scheduling and enrollment of study subjects, obtaining informed consent, and data/sample collection. Coordinates enrollment with health center manager and/or patient care team lead. May also involve providing direct patient care, assisting clinicians and performing components of medical workup as needed, (if qualified) including obtaining blood and urine specimens and the processing and shipping of blood, urine, and swab specimens. Responsible for all study data collected, including completing data collection and entry, and ensuring the quality of case report forms and source documents. Works collaboratively with Health Center staff on integrating study into flow of clinics and coordinate health center assistance with recruitment and enrollment while on-site. Acts as the primary or lead study coordinator for specific clinical trials, including IVD sample collection, medical devices, and drug studies. As lead study coordinator:

Coordinates study start up, training, and documentation necessary for regulatory compliance. Overseeing daily logistics and study operations across multiple health centers, supporting research activities in those sites. Assists with staff training on study protocols, informed consent and any other study tasks. Creating source documents and recruitment materials as needed for study under the guidance of the Clinical Research Manager. Maintains regular communication with sponsors, CROs, and IRBs. Completes IRB submissions and documentation such as applications, continuing reviews and closeouts. Maintains communication with PI for PI oversight responsibilities and documents appropriately. Maintains study files, regulatory documents, and databases and tracks study related correspondence. Manages supplies and ordering for study ensuring adequate supply to maintain enrollment pace and complete projects on timeline.